Study Exploring Safety, Pharmacokinetic and Pharmacodynamic of BN82451 in Male Huntington’s Disease Patients
- 05 February 2025 - 1 mins read
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of BN82451B versus placebo after oral administration twice daily (bid) for 28 days in patients with Huntington’s Disease (HD).
05 February 2025
1 mins read
Which is the Best Dose of Dysport in Helping With Hip Pain for Children With Cerebral Palsy?
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Study to Assess Impact of Dysport Injections Early After Stroke on Upper Limb Spasticity Progression
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Efficacy and Safety Study of Botulinum Toxin Type-A (Dysport®) in Continent Female Subjects Suffering From Idiopathic Overactive Bladder
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Dysport® Pediatric Lower Limb Spasticity Follow-on Study
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Dysport® Adult Lower Limb Spasticity Follow-on Study
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Dysport® Pediatric Lower Limb Spasticity Study
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Dysport® Adult Lower Limb Spasticity Study
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Efficacy and Safety of Botulinum Toxin Type A Haemagglutinin Complex Next Generation (BTX-A-HAC NG) in Glabellar Lines
05 February 2025
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Efficacy and Safety of Clostridium Botulinum Toxin Type A to Improve Appearance of Moderate to Severe Glabellar Lines
05 February 2025
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